Efficient stereoselective syntheses of isopanepoxydone and panepoxydone: are-assignment of relative configuration

Authors
Shotwell, JB Hu, SJ Medina, E Abe, M Cole, R Crews, CM Wood, JL
Citation
Jb. Shotwell et al., Efficient stereoselective syntheses of isopanepoxydone and panepoxydone: are-assignment of relative configuration, TETRAHEDR L, 41(49), 2000, pp. 9639-9643
Citations number
14
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
49
Year of publication
2000
Pages
9639 - 9643
Database
ISI
SICI code
0040-4039(200012)41:49<9639:ESSOIA>2.0.ZU;2-C
Abstract
Recent efforts in our laboratories have resulted in efficient racemic synth eses of isopanepoxydone and panepoxydone, secondary metabolites isolated or iginally from the basidiomycete Panus conchatus. These synthetic efforts ha ve led us to assign the structure of isopanepoxydone as that of 3 and re-as sign the structure of panepoxydone as 2. (C) 2000 Elsevier Science Ltd. All rights reserved.